MEET CLARET AT AACR 2026

CFDNA METHYLATION AND FFPE GENOMIC PROFILING

Built for real-world samples

Attending AACR? Connect with us to discuss robust workflows for challenging samples - from low-input cfDNA methylation and fragmentomics to degraded FFPE DNA and RNA sequencing.

👉 Schedule a meeting here

👉 Or email HERE

Who Should Meet Us

We’re meeting with researchers working on:

cfDNA methylation and fragmentomics
Early-stage cancer research workflows
FFPE-based sequencing and biomarker discovery
Low-input or degraded DNA challenges

cfDNA Methylation (SRSLY MethylPlus)

High-quality methylation data starts upstream

SRSLY MethylPlus is designed for cfDNA workflows where input is limited and fragmentation patterns matter. It enables efficient library preparation while preserving the integrity of methylation signals and cfDNA fragmentomics.

Optimized for low-input cfDNA
Compatible with enzymatic conversion workflows
Supports high-complexity libraries for fragmentomics + methylation analysis

Workflow flexibility matters
SRSLY MethylPlus is validated for compatibility with enzymatic conversion methods, including NEB’s EM-Seq v2.

FFPE Genome Profiling (ForShear + SRSLY)

FFPE doesn’t have to limit your data

Degraded DNA from FFPE samples remains one of the biggest bottlenecks in cancer genomics. Our workflow enables more complete and reliable genome profiling from challenging inputs.

Improved recovery from degraded DNA
Supports whole genome and structural variation analysis
Designed for reproducibility across variable FFPE quality

AACR 2026